For the past two months, Hannah has been battling a life altering, rare neurological autoimmune disease called Myasthenia Gravis. It is caused by a breakdown in the communication between nerves and muscles in mostly the face, eye, throat, arms, and legs. This disease unfortunately has no cure and can be quite debilitating.

Hannah has been in the hospital, mostly the ICU, for the past two months now. She has undergone 5 intubations, multiple ventilators, a tracheostomy, endless feeding tubes and blood work, and finally had a PEG tube placed on her stomach. She has been through challenge after challenge and had even went into cardiac arrest and fought her way back because she is STRONG. Because of her disease, she will most likely not be able to return to a full time job, or job in general for quite some time. Her insurance covered most of her hospital stay, but now that she is stable, she is being moved to an LTAC Rehab Facility that is not covered by her insurance and we are trying to work around that. Her journey has been long, painful, and stressful. She had to give up her summer with her daughter to take care of herself, so let’s help take care of her a little. Please donate if you can and share Hannah’s story.